FDA 510(k)

ANSPACH DISSECTION TOOLS

K-Number: K113476 · 2011-12-16

Decision Date2011-12-16

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ANSPACH DISSECTION TOOLS is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 2011-12-16 under 510(k) number K113476. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSPACH DISSECTION TOOLS?

ANSPACH DISSECTION TOOLS is a medical device that received FDA 510(k) clearance on 2011-12-16. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K113476.

When did ANSPACH DISSECTION TOOLS receive FDA 510(k) clearance?

ANSPACH DISSECTION TOOLS received FDA 510(k) clearance on 2011-12-16, under 510(k) number K113476.

Who is the listed applicant for ANSPACH DISSECTION TOOLS?

The FDA 510(k) record lists The Anspach Effort, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANSPACH DISSECTION TOOLS?

The FDA product code for ANSPACH DISSECTION TOOLS is HBE.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.